The RDA does not apply at all for minerals, its illogical given the various salts...beyond elemental dosing. The variance in Biovailability of the various salts is radical. For example, Lithium orotate when given at the same dose as the lithium carbonate is toxic. It has up to 20 times more bio- than other salts. The orotate vs. carbonate study with lithium showed over 300% the levels...with elementally equivalent amounts. Over 97% of the Lithium orotate is efficacious with studies. Meaning 97% of the elemental gets there.
http://mysite.verizo...ithium-orotate/Orotic Acid boosts muscle phosphocreatine more effectively than just using creatine alone because it increases muscle Uridine levels.
Phosphocreatine fuels ATP and muscular contractions. Elevation of intramuscular Uridine levels increase muscle phosphocreatine and creatine levels in the cardiac tissue.
Orotic Acid can increase ATP production 3 different ways; through the production of ribose moieties, Uridine monophosphate and glycogen storage (elevated glycogen lead to an enhanced capacity for ATP resynthesis from anaerobic glycolysis).
Dr. Hans Nepier, famed German Oncologist. His decades of groundbreaking research included Orotic Acid (uracil-6-carboxylic acid) bound to salts in the sixties. He concluded that orotate salts, being neutrally charged, pass easily through cell membranes.
In effect, orotate shuttles the mineral atoms into cells and tissues, producing higher concentrations. Considering the poor bioavailability of minerals and the mounting research in there relation to optimal athletic performance, Eastern Bloc athletes quickly adopted them with the magnesium orotate gathering much attention.
It wasn't until the 1980's that American researchers started to do clinical studies using magnesium orotate, labeled by researchers as magnerot.
Recently, at the Hamburg symposium on magnesium orotate, a number of studies of metabolic supplementation were presented. Literally hundreds of studies are now published on orotic acid/orotate.
OA has antioxidant properties, which in part explains the protective effects seen neuronally and in the myocardium. OA has ascertained to stimulate erythropoiesis and leucopoiesis... So, do you think increased ATP production, greater oxygenation of the tissues, improved neuronal impulses for reflexes... do you see where this is going in terms of benefit to the individual?
SOOOOOOOOOOOOOOOOOOOOO...elemental. Blah. Read the studies on magnesium orotate and go by those. Again OA is great on its own and synergistic with Magnesium...further it greatly improves the absoprtion and bioavailability to the target tissue. To the point of being a radical difference. Some of these salts, for example, oxide (MagOx was mentioned) have been shown to be vastly inferior.
Carbonate falls very low on the list, nearly as bad as oxide. Hence, you shouldn't just focus on milligrams (although with all the prop. blends in the industry its not an option) and consider bioavailability and how much your body will USE. In many cases compensating by taking more of a poor BV mineral salt is not the best way either. Consider copper and iron in excess can be prooxidant. Many studies on Lithium Orotate or Magnesium Orotate vs. other salts show much more positive effects at drastically lower doses, like 1/8-1/12 the amounts. Hence, lithium when delivered the orotic acid salt would be the preferred form.
Basically Chelates and Orotates are my favorites. Read below. This shows the greatness of the cheapest form of magnesium.
Magnes Res. 2003 Sep;16(3):183-91.
Mg citrate found more bioavailable than other Mg preparations in a randomised, double-blind study.
Walker AF, Marakis G, Christie S, Byng M.
Hugh Sinclair Unit of Human Nutrition, School of Food Biosciences, The University of Reading, Whiteknights, Reading, UK. a.f.walker@reading.ac.uk
Published data on the bioavailability of various Mg preparations is too fragmented and scanty to inform proper choice of Mg preparation for clinical studies. In this study, the relative bioavailability of three preparations of Mg (amino-acid chelate, citrate and oxide) were compared at a daily dose of 300 mg of elemental Mg in 46 healthy individuals. The study was a randomised, double-blind, placebo-controlled, parallel intervention, of 60 days duration. Urine, blood and saliva samples were taken at baseline, 24 h after the first Mg supplement was taken ('acute' supplementation) and after 60 days of daily Mg consumption ('chronic' supplementation). Results showed that supplementation of the organic forms of Mg (citrate and amino-acid chelate) showed greater absorption (P = 0.033) at 60 days than MgO, as assessed by the 24-h urinary Mg excretion. Mg citrate led to the greatest mean serum Mg concentration compared with other treatments following both acute (P = 0.026) and chronic (P = 0.006) supplementation. Furthermore, although mean erythrocyte Mg concentration showed no differences among groups, chronic Mg citrate supplementation resulted in the greatest (P = 0.027) mean salivary Mg concentration compared with all other treatments. Mg oxide supplementation resulted in no differences compared to placebo. We conclude that a daily supplementation with Mg citrate shows superior bioavailability after 60 days of treatment when compared with other treatments studied.
Lastly, this study shows MgO above all other forms of the mineral salt for magnesium is the most pro-oxidant (creating free radical damage) vs. other forms (some others lessen). Not good.
http://www.sci.u-sze...ctaHP/47107.pdfHence, my dislike for Magnesium Oxide.
Hope this helps, as for my rationale.